Canonical Allele Identifier: PA2827989568
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140800
ClinVar RCV Id: RCV000128974 RCV000409539 RCV000481415 RCV000656750 RCV001731385 RCV003407537 RCV003764862 RCV003997468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp2449Asn
CA013697
NM_001354900.2:c.7345G>A